Comparison of location and binding for the positively charged 1,4-dihydropyridine calcium channel antagonist amlodipine with uncharged drugs of this class in cardiac membranes

The distinctive pharmacokinetic and pharmacodynamic activity of amlodipine, including long onset and duration of activity as a calcium channel antagonist, may be related to its interactions with membranes. We have used X-ray crystallography and small-angle X-ray scattering to examine and compare the...

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Veröffentlicht in:Molecular pharmacology 1989-10, Vol.36 (4), p.634-640
Hauptverfasser: MASON, R. P, CAMPBELL, S. F, SHOU-DAO WANG, HERBETTE, L. G
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Sprache:eng
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